class ii alpha
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Author(s):  
D.N. Olivieri ◽  
S. Mirete-Bachiller ◽  
F. Gambón-Deza

AbstractGenes of the major class I and II histocompatibility complex have been extensively studied in mammals. Studies of these antigens in reptiles are very scarce. Here we describe the characteristics of these genes in the suborder Serpentes. We identified the presence of a much larger number of molecules of class I and beta chains of class II than found in mammals. Snakes only have one gene for the class II alpha chain. In these species, class I genes can be classified into two types. Approximately half of the genes lack 10 amino acids in the α1 domain, producing a structural alteration in the interaction region with the T lymphocyte receptor. In the genome of Thamnophis elegans, two haplotypes of an individual were studied revealing a different number and location of class I genes between these haplotypes. The results indicate that in these species, the diversity in the MHC is generated by the presence or absence of genes, independent of the presence of alleles.



2018 ◽  
Vol 71 (2) ◽  
pp. 343-351.e4 ◽  
Author(s):  
Haibin Wang ◽  
Wen-Ting Lo ◽  
Andreja Vujičić Žagar ◽  
Federico Gulluni ◽  
Martin Lehmann ◽  
...  




2017 ◽  
Vol 48 (3) ◽  
pp. 370-372
Author(s):  
Kate L. Ciborowski ◽  
William C. Jordan ◽  
Carlos García de Leániz ◽  
Sofia Consuegra


2016 ◽  
Vol 90 (18) ◽  
pp. 8360-8371 ◽  
Author(s):  
William S. Polachek ◽  
Hanan F. Moshrif ◽  
Michael Franti ◽  
Donald M. Coen ◽  
Vattipally B. Sreenu ◽  
...  

ABSTRACTHigh-throughput small interfering RNA (siRNA) screening is a useful methodology to identify cellular factors required for virus replication. Here we utilized a high-throughput siRNA screen based on detection of a viral antigen by microscopy to interrogate cellular protein kinases and phosphatases for their importance during human cytomegalovirus (HCMV) replication and identified the class II phosphatidylinositol 3-kinase class II alpha (PI3K-C2A) as being involved in HCMV replication. Confirming this observation, infected cells treated with either pooled or individual siRNAs targetingPI3K-C2AmRNA produced approximately 10-fold less infectious virus than the controls. Western blotting and quantitative PCR analysis of infected cells treated with siRNAs indicated that depletion of PI3K-C2A slightly reduced the accumulation of late but not immediate early or early viral antigens and had no appreciable effect on viral DNA synthesis. Analysis of siRNA-treated cells by electron microscopy and Western blotting indicated that PI3K-C2A was not required for the production of viral capsids but did lead to increased numbers of enveloped capsids in the cytoplasm that had undergone secondary envelopment and a reduction in the amount of viral particles exiting the cell. Therefore, PI3K-C2A is a factor important for HCMV replication and has a role in the production of HCMV virions.IMPORTANCEThere is limited information about the cellular factors required for human cytomegalovirus (HCMV) replication. Therefore, to identify proteins involved in HCMV replication, we developed a methodology to conduct a high-throughput siRNA screen of HCMV-infected cells. From our screening data, we focused our studies on the top hit from our screen, the lipid kinase phosphatidylinositol 3-kinase class II alpha (PI3K-C2A), as its role in HCMV replication was unknown. Interestingly, we found that PI3K-C2A is important for the production of HCMV virions and is involved in virion production after secondary envelopment of viral capsids, the encapsidation of HCMV capsids by a lipid bilayer that occurs before virions exit the cell.







2011 ◽  
Vol 63 (6) ◽  
pp. 395-395
Author(s):  
Daniela Gómez ◽  
Pablo Conejeros ◽  
Sergio H. Marshall ◽  
Sofia Consuegra


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